US3408414A - Novel processes and intermediates - Google Patents

Description

United States Patent 0 NOVEL PROCESSES AND INTERMEDIATES Joseph Donald Surmatis, West Caldwell, N.J., assignor to Hoffmann-La Roche Inc., Nutley, N .J., a corporation of New Jersey N0 Drawing. Filed Dec. 4, 1964, Set. Nb. 416,128 10 9 Claims. (Cl. 260-666) 3,408,414 I Patented Oct. 29, 1968 i ABSTRACT OF THE DISCLOSURE A process for preparing'trans-,B-carotene from oXenin or isooxenin by means of reaction with a phosphine or phosphite and intermediates formed in thisprocess.

The instant invention relates to processes and intermediates for the preparation of trans-,B-carotene. More particularly, it relates to processes 'and intermediates for the preparation of'trans-flwarotene from oxen inand isooxenin. 1

The processes of the invention are carried out according to the following reaction scheme:

(I) oxenin 9-[ ,6-trimethy1-1- (II) iaooxenin (cznsom X9 3mm:

+vitam1n A aldehyde H2 (mndlav catalyst) (VI) ll-fiehydro-fi-carotene (VII) ll-mono-ci 5-pcarotene (Ell) 'trans-fi-carotene (IX) retinyl Methyl pho ephonate In the above fiowsheet X is chlorine or bromine, Ar is an aryl radical, e.g., phenyl, monoor dihydroxy-substituted phenyl, or monoor di-lower alkyl-substituted phenyl, e.g., tolyl, xylyl, etc., and R and R are Ar or higher alkyl, i.e., straight or branched chain alkyl having 8 or more carbon atoms.

In the above reaction scheme oxenin (9-[2,6,6-trimethyl 1 cyclohexen 1 yl]-3,7-dimethyl-2,7-nonadien-4- yne-1,6-diol) (I) is reacted with a phosphorus trihalide, i.e., phosphorus tribromide or phosphorus trichloride, to give 9-[2,6,6-trimethyl-l-cyclohexen l yl] 3,7 dimethyl 2,6 nonadien-4-yne-1,8-dihalide (III). Alternatively, isooxenin (9 [2,6,6 trimethyl 1 cyclohexenl-yl]-3,7-dimethyl-1,7-nonadien-4-yne3,6-diol) (II) when reacted with phosphorus trihalide also forms compound (III). The above reactions with phosphorus trihalide are preferably carried out in an inert organic solvent, e.g., a hydrocarbon solvent, such as petroleum ether.

The above dihalide (III) can then be condensed with a phosphine of the formula:

Triphenyl-phosphine is preferred for use in the instant process. This reaction produces a compound of Formula IV.

The compound of Formula IV is then reacted with vitamin A aldehyde, preferably in an inert solvent, e.g., an aliphatic hydrocarbon solvent, benzene, etc., or an ether, e.g., tetrahydrofuran, or in pyridine, the latter being the preferred solvent for use in the practice of the invention, to form ll-dehydro-fl-carotcne (VI). The reaction is carried out in the presence of an alkali metal lower alkoxide, e.g., sodium methoxide. ll-dehydro-fl-carotene (VI) is then hydrogenated in the presence of a palladium catalyst poisoned with lead [see, e.g., H. Lindlar, Helv. Chim. Acta, 35, 446 (1952)], preferably in an inert solvent, e.g., an aliphatic hydrocarbon solvent, to form 11- mono-cis-B-carotene (VII).

ll-mono-cis-fi-carotene is isomerized to trans-p-carotene (VIII) by heating, e.g., at a temperature in the range of from about 90 to about 95 for from about to about hours.

Alternatively, Compound III above can be reacted with triethoxy phosphite to form a phosphonate derivative of Formula V. Compound V is then reacted with vitamin A aldehyde under the same conditions given above for Compound IV to form ll-dehydro-fl-carotene (VI).

Alternatively, Compound V can be hydrogenated with a Lindler catalyst, under the same conditions employed to hydrogenate ll-dehydro-fi-carotene (VI) to ll-monocis-fl-carotene (VII). Retinyl diethyl phosphonate (IX) is formed thereby. Retinyl diethyl phosphonate is then treated with vitamin A aldehyde, under the same conditions employed above with Compound IV, to yield trans- B-carotene (VIII).

Isooxenin (II) is a novel compound which is obtained by reacting 3 hydroxy 3 methyl-pentene-1-yne-4 with methyl magnesium bromide to form the corresponding Grignard compound, and then reacting the latter with 4-(2,6,6 trimethyl cyclohexene-l-yl)-2-methyl-2-butenl-al. The resulting reaction product is decomposed, e.g., with water containing ammonium chloride, acetic acid, or a dilute mineral acid, e.g., HCl, H 80 etc., to yield isooxemn.

The invention will be better understood by reference to the following examples which are given for illustration purposes only and are not meant to limit the invention.

EXAMPLE l.-PREPARATION OF 9 [2,6,6 TRI- METHYL 1 CYCLOHEXEN 1 YL] 3,7 DI- METHYL-2,6-NONADIEN-4-YNE-1,8-HALIDE Oxenin (9 [2,6,G-trimethyl-l-cyclohexen-1-yl]-3,7-dimethyl-2,7-nonadien-4-yne-1,6-diol) (400 g.) was placed in a five liter flask with 2000 ml. of ethyl ether and 5 ml. of pyridine. Phosphorus tribromide (128 ml.) was dissolved in petroleum ether (800 ml.) and added to the stirred reaction at 5 over three hours. The reaction mixture was poured onto crushed ice in a separator, and the ether layer containing the product was separated. This was washed with water. After drying over anhydrous sodium sulfate, the solvent was removed under vacuum, with a temperature not exceeding 30. The product, 9 [2,6,6 trimethyl-l-cyclohexen-l-yl] -3,7-dimethyl-2,6- nonadien-4-yne-l,S-halide, which was obtained as a dark orange colored syrup, weighed 497 g. and the ultraviolet adsorption had a maximum at 287 m (in ethanol).

EXAMPLE 2.-PREPARATION OF TRIPHENYL 9- [2,6,6 TRIMETHYL 1 CYCLOHEXEN 1 YL]- 3,7 DIMETHYL-2,6,8-NONATRIEN-4-YNE PHOS- PHONIUM BROMIDE g. of 9-[2,6,6-trimethyl-l-cyclohexen-l-yl]-3,7-dimethyl-2,6-nonadien-4-yne-1,8-ha1ide, 1000 ml. of tetrahydrofuran, and 167 g. of triphenyl-phosphine were placed in a two-liter flask and stirred under an atmosphere of nitrogen for 48 hours. The ultraviolet adsorption spectrum was determined on a sample of the reaction mixture and was found to have a maximum at 330 me. This was used for the next step without further purification.

EXAMPLE 3.PREPARATION OF ll-DEHYDRO- fl-CAROTENE A methanol solution of sodium methoxide (prepared by dissolving 16 g. of sodium in 500 ml. of methyl alcohol) and a second solution consisting of 77 g. of vitamin A aldehyde dissolved in 500 ml. of methyl alcohol, were charged to separate dropping funnels and added at the same time to the reaction product from Example 2. The addition required one hour. The stirring was then continued for an additional two hours under an atmosphere of nitrogen. The reaction mixture was placed in a separator with one liter of water and extracted with methylene chloride. On removal of the solvent under vacuum, the product consisted of crude ll-dehydro-fl-carotene. The ultraviolet spectrum showed the main adsorption maximum at 427 m with an inflection at 455 m (in cyclohexane). After purification from methylene chloride- .methanol, the product was obtained as an orange colored crystalline solid with lZz. 1800 at 427 m, (in cyclohexane).

EXAMPLE 4.PREPARATION OF ll-MONO- CIS-B-CAROTENE A solution of ll-dehydro-fl-carotene prepared according to Example 3 (10 g.) in n-heptane (200 ml.) was hydrogenated in the presence of 0.5 g. of a lead poisoned palladium catalyst prepared by adding 3.5 parts of lead acetate to 41 parts of palladium chloride precipitated on calcium carbonate (5% palladium chloride) until a one molar equivalent of hydrogen was consumed. The catalyst was filtered off under an atmosphere of nitrogen, and washed with additional n-heptane. On removal of the solvent, the product consisted of crude ll-mono-cis- B-carotene with ultraviolet adsorption maxima at 335, 454, and 480 mp.

EXAMPLE 5.PREPARATION OF TRANS-[3- CAROTENE The 11 mono cis ,8 carotene prepared according to Example 4 was placed in a flask with 20 ml. of heptane 2219 at 454 m... On recrystallization from methylene chloride, pure trans-fi-carotene was obtained with 2450 at 454 mp. (in cyclohexane).

EXAMPLE 6.-PREPARATION oF- DIETHYL 9- [2,6,6-TRIMETHYL 1 CYCLOHEXEN-1-YL]'-3',7- 'DIMETHYL 2,6,8 NONATRIEN 4 YNE PHOS- PHONATE 214 g. of 9-[2,6,6-trimethyl l-cyclohexen-l-yl]-5,7 dimethyl-2,6-nonadien-4-yne-1,8-halide prepared according to Example 1, was placed in a flask with 166 g. of triethyl phosphite. The flask was fitted with a condenser fo'r distillation and the contents were slowlyheated to 140" over a period of two hours. Most of the reaction took place between 120-140", while a distillate which was rich in ethyl bromide was collected. The heating was then continued for an additional hour allowing the temperature to rise to 150.

The lower boiling impurities were removed under vacuum by heating to 120 at mm. There was obtained 216 g. of crude diethyl 9-[2,6,6-trimethyl-l-cyclohexenl-yl]-3,7-dimethyl-,2,6,8-nonatrien 4 yne phosphonate with n 1.5612. A pure analytical sample was prepared by distillation through a molecular still. This had a boiling point of 110 at 10 microns with n 1.5644. The ultra-violet adsorption spectrum had a maximum at 318 m (in ethyl alcohol).

EXAMPLE 7.PREPARATION OF ll-DEHYDRO-fl- CAROTENE 8 g. of diethyl 9-[2,6,6-trimethyl-1-cyclohexen-l-yl]- 3,7-dimethyl-2,6,8-nonatrien-4-yne phosphonate prepared according to Example 6, was dissolved in 100 ml. of tetrahydrofuran. Vitamin A aldehyde (5 g.) and solid sodium methoxide (1.5 g.) were added in the order named. The reaction was stirred under an atmosphere of nitrogen for four hours.

The reaction mixture was diluted with 200 ml. of water and extracted with methylene chloride. After removal of the methylene chloride, the product consisted of 11- dehydro-fi-carotene (which was also obtained by Example 3). The product, after purification from methylene chloride and methyl alcohol, was obtained as an orange colored crystalline solid with Era...

1850 at 427 Ill 1..

EXAMPLE 8.-PREPARATION OF 9 [2,6,6 TRI- METHYL-1-CYCLOHEXEN1-YL]-3 ,7-DIMETHYL- 2,7-NONADIEN-4-YNE-l,6-DIOL One mole of ethyl magnesium bromide in 500 ml. of ethyl ether was prepared by the usual Grignard procedure in a two-liter round-bottom flask. 3-hydroxy-3-methylpenten-1-yne-4 (48 g.) was placed in a separatory funnel with an equal volume of ethyl ether and added to the Grignard reagent over a period of two hours. After stirring for an additional 10 minutes, 103 g. of C aldehyde (4-[2,6,6-trimethylcyclohexen 1 yl]-2-methyl-2- buten-l-al) was charged to the separatory funnel and added while stirring vigorously in one hour. After all of the aldehyde was added, the reaction flask was warmed externally to cause the ether to reflux while stirring for two additional hours.

The reaction was decomposed with water and most of the resulting grey precipitate was dissolved in 5% sulfuric acid. The ether layer-was separated and water washed. On removal of the ether solvent, a white crystalline mass was obtained. To this there was added 200 ml. of petroleum ether. The solid mass was broken up, andthe petroleum ether was heated to reflux while stirring. The solubility of the isooxenin was such that most of it remained undissolved. This was cooled overnight in a refrigerator and filtered. There was obtained 121 g. of dried isooxenin, melting point l02-.

EXAMPLE 9.-PREPARATION OF 9 [2,6,6 TRI- METHYL 1 CYCLOHEXEN 1 YL] 3,7 DI- METHYL 2,6 NONADIEN- 4 YNE 1,8- V'HALIDE I 33 g. of isooxenin which was prepared according to Example 8, was placed in a flask with 200 ml. of ethyl ether and 4 drops of pyridine. Phosphorus tribromide (11 ml.) wasdissolved in 50 ml. of hexane and dropped into the s tirred reaction at 5.in, one hour. The reaction mixture was poured onto crushed ice in a separator. The ether layer was separated, washed with water, saturated sodium bicarbonate solution, and finally with 'water. The solution was dried over anhydrous sodium sulfate, and the solvent was removed under vacuum. The product was obtained as an orange colored syrup, with the violet adsorption maximum at 287 m (in ethanol). This product, 9-[2,6,6-trimethyl-l-cyclohexen-l-yl] 3,7 dimethyl-2,6- nonadien-4-yne-1,8-halide, was identical with the compound prepared according to Example 1.

EXAMPLE IO.PREPARATION OF RETINYL DI- ETHYL PHOSPHONATE A solution of diethyl 9-[2,6,6-trimethyl-l-cyclohexen- 1-yl]3,7-dimethyl-2,6,8-nonatrien-4-yne phosphonate (12 g.) in toluene (240 ml.) was hydrogenated in the presence of poisoned palladium catalyst [H. Lindlar, Helv. Chim. Acta, 35, 446 (1952)] until a one molar equivalent of hydrogen was consumed. The catalyst was filtered off and washed with toluene. Upon removal of the solvent under vacuum, the product, which was retinyl diethyl phosphonate, was obtained as an orange colored syrup with n 1.555. This was employed in the next step without further purification.

EXAMPLE ll.-PREPARATION OF TRANS-fi- CAROTENE Retinyl diethyl phosphonate (10 g.), vitamin A aldehyde (7 g.) and sodium methoxide (1.5 g.) were added to ml. of tetrahydrofuran in the order named and the reaction was stirred under an atmosphere of nitrogen for four hours.

The resulting dark red solution was poured into water and extracted with methylene chloride. On removal of the solvent, the residue consisted of a mixture of trans and ll-mono-cis-B-carotene.

The crude carotene mixture was placed in a flask with 20 ml. of heptane and refluxed for 20 hours under an atmosphere of nitrogen. This was cooled, diluted with additional heptane and filtered to give almost pure transfl-carotene in high yield. On recrystallization from methylene chloride, pure trans-B-carotene was obtained, melting point 182 E2... (454 m 2450 (in cyclohexane).

What is claimed is:

1. A process for the preparation of trans-B-carotene comprising the steps of (a) reacting a compound selected from the group consisting of 9-(2,6,6-trimethyl-l-cyclohexen-1-yl)-3,7-dimethyl 2,7 nonadien-4-yne-1,6-diol and 9(2,6,6-trimethyl l cyclohexen-l-yl)-3,7-dimethyl-2,7-nonadien-4-yne-3,6-diol with a compound selected from the group consisting of phosphorus trichloride and phosphorus tribromide to form 9 (2,6,6-trimethyl-1-cyc1ohexen-1-yl)-3,7-dimethyl 2,6 nonadien 4 yne-1,8-di- 7 halide; (b) reacting 9-(2,6,6-trimethyl 1 cyclohexen-lyl)-3,7-dimethyl-2,6-nonadien 4 yne-1,8-dihalide with a phosphine of the formula:

Ar P 3 wherein Ar is an aryl radical and R and R are selected from the group consisting of higher alkyl and Ar to form a compound of the formula:

wherein Ar, R and R are as above and X is chlorine or bromine (c) reacting a compound of Formula IV with vitamin A aldehyde to form ll-dehydro-fi-carotene; (d) hydrogenating ll-dehydro-fl-carotene in contact with a lead poisoned palladium catalyst to form ll-mono-cis-fi-carotene; and (e) heating ll-mono-cis-B-carotene to form trans-B-carotene.

2. A process according to claim 1 wherein step (a) is carried out with phosphorus tribromide, step -(b) is carried out with triphenyl-phosphine, step (c) is carried out in an inert solvent, and step (e) is carried out in a temperature in the range of from about 90 to about 95 C.

3. ll-dehydro-B-carotene.

4. ll-mono-cis-B-carotene.

5. A process for the preparation of trans-fl-carotene comprising the steps of (a) reacting a compound selected from the group consisting of 9-(2,6,6-trimethyl-l-cyclohexen-l-yl)-3,7-dimethyl 2,7 nonadien-4-yne-l,6-diol and 9-(2,6,6-trimethyl-l-cyclohexen-l-yl) 3,7 dimethyl-2,7-nonadien-4-yne-3,6-diol with a compound selected from the group consisting of phosphorus trichloride and phosphorus tribromide to form 9-(2,6,6-trimethyl-l-cyclohexen-l-yl)-3,7-dimethyl 2,6 nonadien 4 yne-1,8-dihalide; -(b) reacting 9-(2,6,6-trimeth-yl-1-cyc1oheXen-yl)- 3,7-dimethyl 2,6 nonadien-4-yne-l,8-dihalide with triethyl-phosphite to yield diethyl 9-(2,6,6-trimethyl-l-cyclohexen-1-yl)-3,7-dimethyl 2,6,8 nonatrien-4-yne phosphonate; (c) reacting diethyl 9-(2,6,6-trimethyl-1-cyclohexen-l-yl)-3,7-dimethyl- 2,6,8 nonatrien-4-yne phosphonate with vitamin A aldehyde to form ll-dehydro-flcarotene; (d) .hydrogenating ll-dehydro-fl-carotene in contact with a Lindlar catalyst to form' ll-mono-cis-B- carotene; and (e) heating ll-mono-cis-fi-carotene to form trans-,B-carotene.

6. A process according to claim 5 wherein step (a) is carried out with phosphorus tribromide, step (c) is carried out in contact with an inert solvent and step (e) is carried out in the temperature in the range of from about C. to about C.

7. A process for the preparation of trans-fl-carotene' comprising the steps of (a) hydrogenating diethyl 9-(2, 6,6-trimethyl l cyclohexen-l-yl) 3,7 dimethyl-2,6,8- nonatrien-4-yne phosphonate in contact with a Lindlar catalyst to form retinyl diethyl phosphonate and (b) reacting retinyl diethyl phosphonate with vitamin A aldehyde to form trans-pcarotene.

8. A process according to claim 7 wherein step (b) is carried out in contact with an inert solvent.

9. A process for the preparation of trans-fl-carotene comprising reacting retinyl diethyl phosphonate with vitamin A aldehyde.

References Cited UNITED STATES PATENTS 1/1960 Oroshnik 260488 7/1960 Stern 260-666 OTHER REFERENCES L. Zechrneister, Cis-Trans Isomeric Carotenoids, Vitamins A and Aryl Polyenes, Academic Press, 1962, pp. 83-84.

0. Isler et al., Carotenoid and Vitamin A Fields from Advances in Organic Chemistry, vol. 4, Interscience, pp.